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. 2022 Jan 4;10(1):105.
doi: 10.3390/microorganisms10010105.

Red Cusk-Eel (Genypterus chilensis) Gut Microbiota Description of Wild and Aquaculture Specimens

Affiliations

Red Cusk-Eel (Genypterus chilensis) Gut Microbiota Description of Wild and Aquaculture Specimens

Jaime Romero et al. Microorganisms. .

Abstract

Chile has promoted the diversification of aquaculture and red cusk-eel (Genypterus chilensis) is one of the prioritized species. However, many aspects of the biology of the species are unknown or have little information available. These include intestinal microbiota, an element that may play an important role in the nutrition and defense of cultured animals for meat production. This study compares the microbiota composition of the intestinal contents of wild and aquaculture fish to explore the microbial communities present and their potential contribution to the host. DNA was extracted from the intestinal content samples and the V4 region of the 16S rRNA gene was amplified and sequenced using the Ion Torrent platform. After the examination of the sequences, strong differences were found in the composition at the level of phylum, being Firmicutes and Tenericutes the most abundant in aquaculture and wild condition, respectively. At the genus level, the Vagococcus (54%) and Mycoplasma (97%) were the most prevalent in the microbial community of aquaculture and wild condition, respectively. The evaluation of predicted metabolic pathways in these metagenomes showed that in wild condition there is an important presence of lipid metabolism belonging to the unsaturated fatty acid synthesis. In the aquaculture condition, the metabolism of terpenoids and polyketides were relevant. To our knowledge, this is the first study to characterize and compare the intestinal microbiota of red cusk-eel (Genypterus chilensis) of wild and aquaculture origin using high-throughput sequencing.

Keywords: Genypterus chilensis; Ophidiidae; Tenericutes; aquaculture; fish; microbiome; microbiota; next-generation sequencing.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Comparison of alpha diversity indexes between wild and aquaculture red cusk-eel. Diversity in the intestinal bacterial community was measured using between wild (green) and aquaculture (blue). (a) Chao1; (b) PD Whole Tree; (c) Shannon index; (d) Simpson index.
Figure 2
Figure 2
Beta diversity analysis of microbiota composition associated to G. chilensis. PCoA analysis of unweighted UniFrac distances of intestinal microbiota associated to different conditions (wild and aquaculture). Blue circles correspond to samples derived from wild fish (n = 4), and red circles correspond to samples from aquaculture fish (n = 4).
Figure 3
Figure 3
Relative abundances of OTU’s at two taxonomic levels in the intestinal microbiota from wild and aquaculture G. chilensis. Histograms of relative abundances at (a) phylum and (b) genus level for all specimens (n = 8) A group represent to aquaculture samples, whereas W group to wild samples.
Figure 4
Figure 4
Characterization of gut microbiota in wild (green) and aquaculture (red) cusk-eel by LEfSe analysis. Histogram of the LDA scores (log10) of differentially abundant bacterial taxa, LDA scores showed the significant difference between the wild and aquaculture samples.
Figure 5
Figure 5
Presumptive functional pathways of the intestinal microbiota from wild and aquaculture red cusk-eel showing significant differences.
Figure 6
Figure 6
Heatmap showing enzymatic activity assessed by API® ZYM system from wild and aquaculture fish.

References

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